| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:25914051-25914337 | Common:3; Rare:123 | ||||
| chr4:26320764-26321028 | Rare:109; Clinvar (benign):1 | ||||
| chr4:37826505-37826735 | Common:6; Rare:83 | ||||
| chr4:38867565-38867822 | Common:2; Rare:87 | ||||
| chr4:39182204-39182543 | Rare:71; Clinvar:1 | ||||
| chr4:39366319-39366416 | Rare:30 | ||||
| chr4:39458843-39459122 | Common:3; Rare:158; Clinvar:1; Clinvar (benign):5 | ||||
| chr4:39527359-39527754 | Common:2; Rare:93 | ||||
| chr4:39638823-39639142 | Common:1; Rare:115 | ||||
| chr4:39698004-39698171 | Common:1; Rare:67 | ||||
| chr4:41256728-41257025 | Common:3; Rare:95; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr4:41934866-41935234 | Common:3; Rare:94 | ||||
| chr4:41990402-41990577 | Common:1; Rare:64 | ||||
| chr4:44678392-44678696 | Common:1; Rare:115 | ||||
| chr4:44726523-44726629 | Rare:43 |